Expression of nano-engineered RNA organelles in bacteria

Designing synthetic biomolecular condensates, or membraneless organelles, offers insights into the functions of their natural counterparts and is equally valuable for cellular and metabolic engineering. Choosing E. coli for its biotechnological relevance, we deploy RNA nanotechnology to design and express non-natural membraneless organelles in vivo. The designer condensates assemble co-transcriptionally from branched RNA motifs interacting via base-pairing. Exploiting binding selectivity, we express orthogonal, non-mixing condensates, and by embedding a protein-binding aptamer, we achieve selective protein recruitment. Condensates can be made to dissolve and reassemble upon thermal cycling, thereby reversibly releasing and re-capturing protein clients. The synthetic organelles are expressed robustly across the cell population and remain stable despite enzymatic RNA processing. Compared with existing solutions based on peptide building blocks or repetitive RNA sequences, these nanostructured RNA motifs enable algorithmic control over interactions, affinity for clients, and condensate microstructure, opening further directions in synthetic biology and biotechnology.

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Publication Details

Journal
Nature Communications
Published
2026-02-14
DOI
https://doi.org/10.1038/s41467-026-69336-w
Primary Topic
Bacterial Genetics and Biotechnology
Type
article
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article

Expression of nano-engineered RNA organelles in bacteria

Masahiro Takinoue, Lorenzo Di Michele, Sabrina Pia Nuccio, Giacomo Fabrini et al.
Nature Communications
Bacterial Genetics and Biotechnology
article

Expression of nano-engineered RNA organelles in bacteria

Masahiro Takinoue, Lorenzo Di Michele, Sabrina Pia Nuccio, Giacomo Fabrini, Layla Malouf, Roger Rubio‐Sánchez, Graham Christie, Dr Milan Dordevic, C. Fan, Pietro Cicuta, Adam Knirsch, Brian Ng
article en

Abstract

Designing synthetic biomolecular condensates, or membraneless organelles, offers insights into the functions of their natural counterparts and is equally valuable for cellular and metabolic engineering. Choosing E. coli for its biotechnological relevance, we deploy RNA nanotechnology to design and express non-natural membraneless organelles in vivo. The designer condensates assemble co-transcriptionally from branched RNA motifs interacting via base-pairing. Exploiting binding selectivity, we express orthogonal, non-mixing condensates, and by embedding a protein-binding aptamer, we achieve selective protein recruitment. Condensates can be made to dissolve and reassemble upon thermal cycling, thereby reversibly releasing and re-capturing protein clients. The synthetic organelles are expressed robustly across the cell population and remain stable despite enzymatic RNA processing. Compared with existing solutions based on peptide building blocks or repetitive RNA sequences, these nanostructured RNA motifs enable algorithmic control over interactions, affinity for clients, and condensate microstructure, opening further directions in synthetic biology and biotechnology.

Nature CommunicationsVol. 17(1)
University of Cambridge (GB), The Francis Crick Institute (GB), Life Science Institute (JP), Japan Research Institute (JP), Imperial College London (GB)
Openalex Percentile: Top 54%
Bacterial Genetics and Biotechnology
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Expression of nano-engineered RNA organelles in bacteria — Masahiro Takinoue, Lorenzo Di Michele, et al. · Nature Communications (2026) | TGRS Research Map | TGRS